Isolation of cDNA clones for fourteen nuclear-encoded thylakoid membrane proteins |
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Authors: | Jochen Tittgen, Jü rgen Hermans, Johannes Steppuhn, Thomas Jansen, Christer Jansson, Bertil Andersson, Rachel Nechushtai, Nathan Nelson Reinhold G. Herrmann |
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Affiliation: | (1) Botanisches Institut der Ludwig-Maximilians-Universität, Menzinger Strasse 67, D-8000 München 19, Germany;(2) Department of Biochemistry, University of Lund, Lund, Sweden;(3) Biology Department, University of California, Los Angeles, CA, USA;(4) Roche Institute of Molecular Biology, Nutley, NJ, USA |
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Abstract: | Summary Spinach cDNA libraries, made from polyadenylated seedling RNA, have been constructed in pBR322 and the expression vector gt11. Recombinant plasmids or phage for 14 intrinsic and peripheral thylakoid membrane proteins and one stromal protein have been identified. They encode components containing antigenic determinants against the lysine-rich 34 kd, the 23 kd and 16 kd proteins all associated with the water-splitting apparatus of the photosystem II reaction center, the ATP synthase subunits gamma, delta and CFo-II, the Rieske Fe/S protein of the cytochrome b/f complex, subunits 2, 3, 5 and 6 of the photosystem I reaction center, plastocyanin, ferredoxin oxidoreductase, chlorophyll a/b-binding apoproteins of the lightharvesting complex associated with photosystem II, and the small subunit of the stromal enzyme ribulose bisphosphate corboxylase/oxygenase. The cDNA inserts lack complementarity to plastid DNA but hybridize to restricted nuclear DNA as well as to discrete poly A+-mRNA species. The precursor products obtained after translation of hybrid selected RNA fractions in a wheat germ assay are imported and processed by isolated unbroken spinach chloroplasts. The imported components comigrate with the respective authentic proteins. |
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